810682-40-7

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 12 carbon (C) atoms, 24 hydrogen (H) atoms, and 3 oxygen (O) atoms.

Explanation

The compound has a spiro (interlocking) structure with a dioxaspiro (two oxygen atoms in a ring) core. It also contains four methyl (CH3) groups as substituents.

Explanation

The stereochemistry describes the spatial arrangement of atoms around the stereocenters. In this case, both the 5th and 7th positions have an S (si) configuration, which means the substituents are arranged in a specific order in three-dimensional space.

Explanation

Due to its unique structure and properties, 1,3-Dioxaspiro[4.5]decan-7-ol,2,2,6,6-tetramethyl-,(5S,7S)-(9CI) may have potential uses in the pharmaceutical and fragrance industries. However, further research is needed to fully understand its potential applications.

Explanation

While the compound has potential applications, more research is required to fully understand its properties, uses, and potential benefits in various industries.

Chemical Structure

Spiroketone with a dioxaspiro core and four methyl substituents

Stereocenters

5th and 7th positions

Stereochemistry

(5S,7S)-configuration

Potential Applications

Pharmaceutical and fragrance industries

Research Status

Further research needed

Upstream product

• 67-64-1 acetone 
• 954096-32-3 (1S,3S)-1-Hydroxymethyl-2,2-dimethyl-cyclohexane-1,3-diol 
• 810682-53-2 (S)-3-(Iodomethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-39-4 (S)-3-(Bromomethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-13-4 (1S,5S)-3,3,9,9-Tetramethyl-2-oxa-3-sila-bicyclo[3.3.1]nonan-5-ol 
• 810682-12-3 (S)-3-(Chloromethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 87655-21-8 (S)-3-hydroxy-2,2-dimethylcyclohexanone 

Downstream Products

• 810682-44-1 Acetic acid (S)-4-(4-methoxy-benzyloxymethyl)-1-methoxymethoxy-2,2-dimethyl-cyclohex-3-enylmethyl ester 
• 810682-45-2 [(S)-4-(4-Methoxy-benzyloxymethyl)-1-methoxymethoxy-2,2-dimethyl-cyclohex-3-enyl]-methanol 
• 810682-17-8 Acetic acid (S)-1-hydroxy-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-cyclohex-3-enylmethyl ester 
• 810682-43-0 (S)-1-Hydroxymethyl-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-cyclohex-3-enol 
• 810682-16-7 (S)-8-(4-Methoxy-benzyloxymethyl)-2,2,6,6-tetramethyl-1,3-dioxa-spiro[4.5]dec-7-ene 
• 810682-41-8 (S)-2,2,6,6-Tetramethyl-8-methylene-1,3-dioxa-spiro[4.5]decan-7-one 
• 810682-15-6 (S)-2,2,6,6-Tetramethyl-8-methylene-1,3-dioxa-spiro[4.5]decan-7-ol 

Relevant academic research and scientific papers

Development of silicon-tethered anionic reaction and its application to the synthesis of chiral A-ring moieties of Taxol

Silicon-tethered intramolecular nucleophilic additions of a hydroxymethyl unit to ketones in β-hydroxyketones have been developed. The product obtained by this protocol was successfully converted to chiral A-ring moieties of Taxol. Also developed was a pr